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Research Coordinator - Smidt Heart Institute

Company: Careerbuilder-US
Location: Los Angeles
Posted on: November 26, 2022

Job Description:

Grow your career at Cedars-Sinai!The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and niche care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.Join our team and use your experience with an organization known nationally for excellence in research!Job Summary: -The Research Coordinator I prepares and submits protocols and supporting documents to regulatory bodies such as the IACUC, and IRB. -This role submits continuations, amendments, responds to questions, generates reports, and maintains research files and documentation involving the regulatory requirements for the study/clinical trial. -Other duties include physical lab management, ordering and stocking of supplies, representing the medical center when meeting with pharmaceutical companies, attending weekly team meetings, and working with other staff to ensure all regulatory documents and requirements are met and up-to-date. -Ensures compliance with all federal and local agencies including the United States Department of Agriculture (USDA) and the American Association for Laboratory Animal Science (AALAC).Primary Duties and Responsibilities:

  • Submits continuations and amendments as vital to maintain compliance with regulatory requirements and institutional policies.
  • Responds to all questions from the IACUC and/or IRB related to the regulatory aspects of the study.
  • Completes forms and generates all reports vital to align with regulatory requirements and institutional policies.
  • Establishes and maintains research files and documentation pertaining to regulatory requirements for pre-clinical trials.
  • Meets with monitors from pharmaceutical companies and represents the medical center during these meetings.
  • Works closely with the Principal investigator, research staff, and regulatory staff to assure that all regulatory documents for the research studies are up-to-date.
  • Participates in weekly research team meetings and updates staff and investigators on the status of regulatory submission and amendments.
  • May be required to develop budgets.
  • Ensures compliance with all federal and local agencies including the USDA and Internal Animal Care and Use Committee and the local Institutional Review Board. -
  • Participates in required training and education programs. Educational Requirements:BA/BS degree required, -Masters or MBA preferredLicenses:N/AExperience:One (1) year directly related experience, or equivalent combination of education & experience.Physical Demands:Able to perform moderate lifting. -Able to sit, stand and walk for prolonged periods of time. -Able to read papers and online documents. -Able to operate standard office equipment. -Able to exercise physical ability and perspective acuity to satisfactorily perform essential job functions. Working Title:Department:Business Entity:Job Category:Job Specialty:Position Type:Shift Length:Shift Type:

Keywords: Careerbuilder-US, Los Angeles , Research Coordinator - Smidt Heart Institute, Other , Los Angeles, California

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